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Albert V Smith

Showing results (91-100 of 271) with videos related to

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Nature Genetics|July 15, 2009
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestryEmelia J Benjamin, Kenneth M Rice, Dan E Arking, et al.
The Lancet. Diabetes & Endocrinology|October 17, 2017
Omega-6 fatty acid biomarkers and incident type 2 diabetes: pooled analysis of individual-level data for 39 740 adults from 20 prospective cohort studiesJason H Y Wu, Matti Marklund, Fumiaki Imamura, et al.
Nature Communications|March 27, 2026
An integrated germline and somatic genomic model for coronary artery diseaseXiong Yang, Min Seo Kim, Xinyu Zhu, et al.
Plos One|May 8, 2020
Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucosePeitao Wu, Denis Rybin, Lawrence F Bielak, et al.
Nature Communications|October 16, 2025
Genetic determinants and genomic consequences of non-leukemogenic somatic point mutationsJoshua S Weinstock, Sharjeel A Chaudhry, Maria Ioannou, et al.
Journal of the American College of Cardiology|February 4, 2014
Novel genetic markers associate with atrial fibrillation risk in Europeans and JapaneseSteven A Lubitz, Kathryn L Lunetta, Honghuang Lin, et al.
Medrxiv : the Preprint Server for Health Sciences|March 4, 2025
Cross-cohort analysis of expression and splicing quantitative trait loci in TOPMedPeter Orchard, Thomas W Blackwell, Linda Kachuri, et al.
Nature Genetics|April 17, 2012
Common variants at 6q22 and 17q21 are associated with intracranial volumeM Arfan Ikram, Myriam Fornage, Albert V Smith, et al.
Scientific Reports|November 9, 2016
Gene-gene Interaction Analyses for Atrial FibrillationHonghuang Lin, Martina Mueller-Nurasyid, Albert V Smith, et al.
Annals of Neurology|June 18, 2011
Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortiumMyriam Fornage, Stephanie Debette, Joshua C Bis, et al.
Pageof 28

Showing results (91-100 of 271) with videos related to

Sort By:
Pageof 28
Nature Genetics|July 15, 2009
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestryEmelia J Benjamin, Kenneth M Rice, Dan E Arking, et al.
The Lancet. Diabetes & Endocrinology|October 17, 2017
Omega-6 fatty acid biomarkers and incident type 2 diabetes: pooled analysis of individual-level data for 39 740 adults from 20 prospective cohort studiesJason H Y Wu, Matti Marklund, Fumiaki Imamura, et al.
Nature Communications|March 27, 2026
An integrated germline and somatic genomic model for coronary artery diseaseXiong Yang, Min Seo Kim, Xinyu Zhu, et al.
Plos One|May 8, 2020
Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucosePeitao Wu, Denis Rybin, Lawrence F Bielak, et al.
Nature Communications|October 16, 2025
Genetic determinants and genomic consequences of non-leukemogenic somatic point mutationsJoshua S Weinstock, Sharjeel A Chaudhry, Maria Ioannou, et al.
Journal of the American College of Cardiology|February 4, 2014
Novel genetic markers associate with atrial fibrillation risk in Europeans and JapaneseSteven A Lubitz, Kathryn L Lunetta, Honghuang Lin, et al.
Medrxiv : the Preprint Server for Health Sciences|March 4, 2025
Cross-cohort analysis of expression and splicing quantitative trait loci in TOPMedPeter Orchard, Thomas W Blackwell, Linda Kachuri, et al.
Nature Genetics|April 17, 2012
Common variants at 6q22 and 17q21 are associated with intracranial volumeM Arfan Ikram, Myriam Fornage, Albert V Smith, et al.
Scientific Reports|November 9, 2016
Gene-gene Interaction Analyses for Atrial FibrillationHonghuang Lin, Martina Mueller-Nurasyid, Albert V Smith, et al.
Annals of Neurology|June 18, 2011
Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortiumMyriam Fornage, Stephanie Debette, Joshua C Bis, et al.
Pageof 28